Canonical Allele Identifier: CA391933826

Gene: SPRED1

Linked Data

• MyVariant Identifiers: chr15:g.38591596G>T (hg19) ; chr15:g.38299395G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.38299395G>T , CM000677.2:g.38299395G>T	GRCh38
NC_000015.9:g.38591596G>T , CM000677.1:g.38591596G>T	GRCh37
NC_000015.8:g.36378888G>T	NCBI36
NG_008980.1:g.51545G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299084.9:c.55G>T MANE Select	ENSP00000299084.4:p.Ala19Ser
ENST00000299084.8:c.55G>T	ENSP00000299084.4:p.Ala19Ser
ENST00000561205.1:n.393G>T
ENST00000561317.1:c.-9G>T	ENSP00000453680.1:n.-9G>T
NM_152594.2:c.55G>T	NP_689807.1:p.Ala19Ser
XM_005254202.2:c.91G>T	XP_005254259.1:p.Ala31Ser
XM_005254203.3:c.-15-22846G>T	XP_005254260.1:n.-15-22846G>T
XM_011521288.1:c.-9G>T	XP_011519590.1:n.-9G>T
XM_011521289.1:c.-9G>T	XP_011519591.1:n.-9G>T
XM_011521290.1:c.-9G>T	XP_011519592.1:n.-9G>T
XM_005254202.3:c.91G>T	XP_005254259.1:p.Ala31Ser
XM_011521289.3:c.-9G>T	XP_011519591.1:n.-9G>T
NM_152594.3:c.55G>T MANE Select	NP_689807.1:p.Ala19Ser